Paper bulking promoter

ABSTRACT

This invention is to provide a paper bulking promoter with which a highly bulky sheet can be obtained without impairing paper strength.  
     Namely, this invention provides a process for producing a bulky paper, comprising the step of making paper from pulp in the presence of a bulking promoter comprising at least one compound selected from the group consisting of a cationic compound, an amine compound, an acid salt of an amine compound, an amphoteric compound, an amide compound, a quaternary ammonium salt, and an imidazoline derivative.

BACKGROUND OF THE PRIOR ART

[0001] 1. Technical Field

[0002] This invention relates to a paper bulking promoter with which the sheets of paper obtained from a pulp feedstock can be bulky without impairing paper strength.

[0003] 2. Description of the Prior Art

[0004] Recently, there is a desire for high-quality paper, e.g., paper excellent in printability and voluminousness. Since the printability and voluminousness of paper are closely related to the bulkiness thereof, various attempts have been made to improve bulkiness. Examples of such attempts include a method in which a crosslinked pulp is used (JP-A 4-185792, etc.) and a method in which a mixture of pulp with synthetic fibers is used as a feedstock for papermaking (JP-A 3-269199, etc.). Examples thereof further include a method in which spaces among pulp fibers are filled with a filler such as an inorganic (JP-A 3-124895, etc.) and a method in which spaces are formed (JP-A 5-230798, etc.). On the other hand, with respect to mechanical improvements, there is a report on an improvement in calendering, which comprises conducting calendering under milder conditions (JP-A 4-370298).

[0005] However, the use of a crosslinked pulp, synthetic fibers, etc. makes pulp recycling impossible, while the technique of merely filling pulp fiber spaces with a filler and the technique of forming spaces result in a considerable decrease in paper strength. Furthermore, the improvement in mechanical treatment produces only a limited effect and no satisfactory product has been obtained so far.

[0006] Also known is a method in which a bulking promoter is added during papermaking to impart bulkiness to the paper. Although fatty acid polyamide polyamines for use as such bulking promoters are on the market, use of these compounds results in a decrease in paper strength and no satisfactory performance has been obtained therewith.

SUMMARY OF THE INVENTION

[0007] The inventors have made intensive investigations in view of the problems described above. As a result, they have found that by incorporating at least one compound selected among specific cat ionic compounds, amine compounds, acid salts of amine compounds, amphoteric compounds, amide compounds, quaternary ammonium salts, and imidazoline derivatives, optionally together with at least one specific nonionic surfactant into a pulp feedstock, e.g., a pulp slurry, in the papermaking step, the sheet made from the feedstock can have improved bulkiness without detriment to paper strength. This invention has thus been achieved.

[0008] Namely, this invention provides a process for producing a bulky paper, comprising the step of making paper from pulp in the presence of a bulking promoter comprising at least one compound selected from the group consisting of a cationic compound, an amine compound, an acid salt of an amine compound, an amphoteric compound, an amide compound, a quaternary ammonium salt, and an imidazoline derivative.

[0009] The term “paper bulking promoter” used herein means an agent with which a sheet of paper obtained from a pulp feedstock can have a larger thickness (can be bulkier) than that having the same basis weight obtained from the same amount of a pulp feedstock.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

[0010] Examples of the cationic compounds for use in this invention include compounds represented by the following formulae (a₁) and (b₁):

[0011] wherein R₁₁ and R₁₂ are the same as or different from each other, and an alkyl, alkenyl or β-hydroxyalkyl group having 8 to 24 carbon atoms; R₁₃, R₁₄ and R₁₅ are the same as or different from each other, and an alkyl or hydroxyalkyl group having 1 to 8 carbon atoms, benzyl or —(AO)n₁₁—Z₁₁ wherein AO is an oxyalkylene unit having 2 or 3 carbon atoms, Z₁₁ is a hydrogen atom or an acyl group and n₁₁ is an integer of 1 to 50; R₁₆ is an alkyl, alkenyl or β-hydroxyalkyl group having 8 to 36 carbon atoms; and X⁻ is an anionic ion.

[0012] In the formula (a₁), R₁₁ and R₁₂, which are the same or different, each preferably is an alkyl or alkenyl group having 10 to 22 carbon atoms. R₁₃ and R₁₄, which are the same or different, each preferably is a hydrogen atom or an alkyl group having 1 to 3 carbon atoms. Examples of X⁻, which is an anionic ion, include hydroxy, halide, and monoalkyl (C1-C3) sulfate ions and anions derived from inorganic or organic acids. X⁻ is preferably a halide ion, especially Cl⁻.

[0013] In the formula (b₁), R₁₃, R₁₄, and R₁₅, which are the same or different, each is preferably an alkyl group having 1 to 3 carbon atoms or a benzyl group. R₁₆ is preferably an alkyl group having 10 to 22 carbon atoms. Examples of the anionic ion X⁻ are the same as those in the formula (a₁). X⁻ is preferably a halide ion, especially Cl⁻.

[0014] In the present invention, the cationic compounds may include quaternary ammonium salts.

[0015] Hereinafter X⁻ may be an anionic ion as an anionic ion.

[0016] Examples of the amine compounds and the acid salts of amine compounds for use in this invention include compounds represented by the following formulae (a₂) to (f₂):

[0017] wherein R₂₁ is an alkyl, alkenyl or βhydroxyalkyl group having 8 to 36 carbon atoms; R₂₂ and R₂₃ are the same as or different from each other, and a hydrogen atom, an alkyl group having 1 to 24 carbon atoms or an alkenyl group having 2 to 24 carbon atoms; R₂₄ and R₂₅ are the same as or different from each other, and a hydrogen atom or an alkyl group having 1 to 3 carbon atoms; HB represents an inorganic acid or an organic acid; AO is an oxyalkylene unit having 2 or 3 carbon atoms; l₂₁ and m₂₁ are 0 or a positive integer, and the sum in total of l₂₁ and m₂₁ is in an integer ranging from 1 to 300; and n₂l is a number of 1 to 4.

[0018] In the formulae (a₂) to (f₂), R₂₁ is preferably an alkyl group having 10 to 22 carbon atoms. R₂₂ and R₂₃, which are the same or different, each preferably is a hydrogen atom or an alkyl group having 1 to 22 carbon atoms. In HB in the acid salts of amine compounds, B is preferably a halogen or a carboxylate having 2 to 5 carbon atoms, especially preferably a carboxylate having 2 or 3 carbon atoms. Preferred amine compounds and preferred acid salts of amine compounds are the compounds represented by the formulae (a₂) and (b₂) respectively.

[0019] The acid salt represented by the formula (b₂) may be signified by the following formula (b₂₁):

[0020] wherein R₂₁, R₂₂ and R₂₃ are same as above-mentioned; H is hydrogen atom; and B⁻ represents a base

[0021] That is, the acid salt may be an ionized compound.

[0022] Examples of the amphoteric compounds for use in this invention include compounds represented by the following formulae (a₃) to (j3):

[0023] wherein R₃₁, R₃₂ and R₃₃ are the same as or different from each other, and an alkyl group having 1 to 24 carbon atoms or an alkenyl group having 2 to 24 carbon atoms; R₃₄ is an alkyl, alkenyl or β-hydroxyalkyl group having 8 to 36 carbon atoms; M is a hydrogen atom, an alkali metal atom, a half a mole of an alkaline earth metal atom or an ammonium group; Y₃₁ is R₃₅NHCH₂CH₂—, wherein R₃₅ is an alkyl group having 1 to 36 carbon atoms, or an alkenyl or a hydroxy alkyl group having 2 to 36 carbon atoms; Y₃₂ is a hydrogen atom or R₃₅NHCH₂CH₂—, R₃₅ being defined above; Z₃₁ is —CH₂COOM, M being defined above; and Z₃₂ is a hydrogen atom or —CH₂COOM, M being defined above.

[0024] In the formulae (a₃) to (j₃), R₃₁, R₃₂, and R₃₃, which are the same or different, each preferably is an alkyl group having 1 to 22 carbon atoms. Especially preferably, R₃₁ is an alkyl group having 10 to 20 carbon atoms, and R₃₂ and R₃₃ each is an alkyl group having 1 to 3 carbon atoms. R₃₄ is preferably an alkyl group having 10 to 22 carbon atoms. Preferred amphoteric compounds are those represented by the formulae (a₃) and (b₃)

[0025] Examples of the other amine compounds and the other acid salts of an amine compound for use in this invention include compounds represented by the following formulae (a₄) to (d₄):

[0026] wherein R₄₁ is an alkyl, alkenyl or β-hydroxyalkyl having 8 to 35 carbon atoms; R₄₃ and R₄₄ are same as or different from each other, an alkyl, alkenyl or β-hydroxyalkyl group having 7 to 35 carbons atoms; R₄₆ is a hydrogen atom or an alkyl group having 1 to 3 carbon atoms; R₄₅ is an alkyl group having 1 to 3 carbon atoms; R₄₂ is a hydrogen atom or R₄₇, wherein R₄₇ is an alkyl, alkenyl or β-hydroxyalkyl group having 7 to 35 carbons atoms; Y₄₁ is a hydrogen or —COR₄₄; and Z₄₁ is —CH₂CH₂O(AO)n₄₁—OCOR₄₇, wherein A is a liner or branched alkylene unit having 2 to 3 carbon atoms, or —CH₂CH(OH)—CH₂OCOR₄₇ and n₄₁is an average added-number ranging 1 to 20.

[0027] Examples of the amide compounds for use in this invention include compounds represented by the following formulae (a₅) and (b₅):

[0028] wherein R₅₁ and R₅₄ are same as or different from each other, an alkyl, alkenyl or β-hydroxyalkyl group having 7 to 35 carbon atoms; R₅₂ and R₅₃ are same as or different from each other, a hydrogen atom or an alkyl group having 1 to 3 carbon atoms; and Y₅₁ and Y₅₂ are same as or different from each other, and a hydrogen atom, R₅₂CO—, R₅₄CO—, —(AO)n₅₁—COR₅₅, wherein A is a liner or branched alkylene unit having 2 to 3 carbon atoms n₅₁ is an average added-number ranging 1 to 20, and R₅₅ is an alkyl, alkenyl or β-hydroxyalkyl group having 7 to 35 carbon atoms, or —(AO)n₅₁—H, wherein A and n₅₁ are defined above.

[0029] Examples of the cationic compounds for use in this invention include quaternary ammonium salts represented by the following formulae (a₆) and (b₆):

[0030] wherein R₆₁ and R₆₃ are same as or different from each other, an alkyl, alkenyl or β-hydroxyalkyl group having 7 to 35 carbons atoms; R₆₅ is a hydrogen atom or an alkyl group having 1 to 3 carbon atoms; R₆₂ and R₆₄ are same as or different from each other, an alkyl group having 1 to 3 carbon atoms; and X⁻ is an anionic ion.

[0031] Examples of the imidazoline derivative for use in this invention include compounds represented by the following formulae (a₇):

[0032] wherein R₇₁ is an alkyl, alkenyl or β-hydroxyalkyl group having 7 to 35 carbons atoms.

[0033] The paper bulking promoter of this invention preferably further contains at least one specific nonionic surfactant. By the use of at least one of compounds represented by the above formulae (a₁) and (b₁), (a₂) to (e₂), (a₃) to (h₃), (a₄) to (d₄), (a₅) and (b₅), (a₆) and (b₆), and (a₇); and at least one specific nonionic surfactant in combination, the effect of this invention can be improved. Examples of the nonionic surfactant for use in this invention include the following (A) to (C).

[0034] (A): a compound represented by the following formula (A)

R₈₁O(EO)_(m) ₈₁ (PO)_(n) ₈₁ H  (A)

[0035] wherein R₈₁ is a C6 to C22 straight or branched alkyl or alkenyl group or an alkylaryl group having a C4 to C20 alkyl group; E is an ethylene unit; P is a propylene unit; m₈₁ and n₈₁ are an average number of added moles, m₈₁ is a number in the range of 0 to 20 and n₈₁ is a number in the range of 0 to 50; and the addition form of EO and PO may be any of block and random and the addition order of EO and PO may be not limited.

[0036] The compounds represented by the formula (A) are ones each obtained by causing a higher alcohol, an alkylphenol, or the like in which the alkyl has 6 to 22 carbon atoms to add an alkylene oxide such as ethylene oxide (EO) or propylene oxide (PO). In this invention is used the compound in which the average number of moles of ethylene oxide added is in the range of 0≦m₈₁≦20. The range of the average number of moles added, m₈₁, is preferably 0≦m₈₁≦10, more preferably 0≦m₈₁≦5. If m₈₁ exceeds 20, the effect of imparting bulkiness to paper is lessened. Further, the compound used is one in which the average number of moles of propylene oxide (PO) added, n₈₁, is in the range of 0≦n₈₁≦50, preferably 0≦n₈₁≦20. When n₈₁ exceeds 50, such a compound is economically disadvantageous although the decrease in performance is little.

[0037] R₈₁ in the formula (A) is preferably a linear or branched, alkyl or alkenyl group having 8 to 18 carbon atoms. If R₈₁ in the formula (A) is an alkyl or alkenyl group in which the number of carbon atoms is outside the range of from 6 to 22 or if R₈₁ is an alkylaryl group in which the number of carbon atoms of the alkyl group is outside the range of from 4 to 20, then the compound is less effective in imparting bulkiness to paper.

[0038] Examples of E and P in the formula (A), which each represents a linear or branched alkylene group having 2 or 3 carbon atoms, include ethylene and propylene. When the group (EO)_(m) ₈₁ (PO)_(n) ₈₁ in the formula (A) is composed of a combination of polyoxyethylene and polyoxypropylene, the C₂H₄O and C₃H₆O units may have any of random and block arrangements (,or the addition form of EO and PO may be any of block and random). In this case, the polyoxypropylene (C₃H₆O) group(s) account for preferably at least 50 mol %, especially preferably at least 70 mol %, of all groups added on the average. The alkylene oxide group bonded to R may begin with any of EO and PO (or the addition order of EO and PO may be not limited).

[0039] (B): Compounds represented by the following formula (B)

R₈₁COO(EO)_(m) ₈₁ (PO)_(n) ₈₁ R_(b)  (B)

[0040] wherein R₈₁, E, P, m₈₁ and n₈₁ are the same as those of the formula (A); and R_(b) is H, an alkyl, an alkenyl or an alkylaryl group.

[0041] Preferred examples of R₈₁, E, P, m₈₁, and n₈₁ in the formula (B) are the same as those in the formula (A). Examples of the alkyl and alkenyl groups represented by R_(b) in the formula (B) include those having 1 to 4 carbon atoms, while examples of the alkylaryl group represented by R_(b) include alkylphenyl groups in each of which the alkyl has 1 to 4 carbon atoms.

[0042] (C): a nonionic surfactant selected from the followings (1) to (3)

[0043] (1) an oil-fat type nonionic surfactant (i.e. a ninionic surfactant based on fat),

[0044] (2) a sugar-alcohol type nonionic surfactant (i.e. a nonionic surfactant based on sugar alcohol) and

[0045] (3) a sugar-type nonionic surfactant (l.e. a nonionic surfactant based on sugar).

[0046] (1) Nonionic Surfactants Based on Fat

[0047] Examples of the nonionic surfactants based on a fat (1) include ones obtained by mixing an alcohol having 1 to 14 hydroxy groups with a fat such as those given in, e.g., JP-A 4-352891 or with a product of the reaction of the fat with glycerol and causing the mixture to add an alkylene oxide (AO) Preferred is one obtained by causing a mixture of a fat and a polyhydric alcohol to add an AO. The AO is ethylene oxide (EO) and/or propylene oxide (PO). In the case of using both EO and PO, the EO/PO polymer may have any of random and block arrangements. The average number of moles of EO added is preferably 0 to 200, more preferably 10 to 100, while that of PO added is preferably 0 to 150, more preferably 2 to 100.

[0048] Examples of the fat usable for this type of nonionic surfactant include land animal fats, marine animal fats, hardened or semihardened oils obtained therefrom, and recovery oils obtained during the purification of these fats. Preferred examples thereof include coconut oil, beef tallow, fish oils, linseed oil, rapeseed oil, and castor oil. In the case where any of these fats is reacted beforehand with glycerol, the fat/glycerol ratio is preferably from 1/0.05 to 1/1.

[0049] Examples of monohydric alcohols among the alcohols having 1 to 14 hydroxy groups usable for this type of nonionic surfactant include linear or branched, saturated or unsaturated alcohols having 1 to 24 carbon atoms and cyclic alcohols. Preferred are linear or branched, saturated alcohols having 4 to 12 carbon atoms. Examples of dihydric alcohols include α,ω-glycols having 2 to 32 carbon atoms, 1,2-diols, symmetric α-glycols, and cyclic 1,2-diols. Preferred are α,ω-glycols having 2 to 6 carbon atoms. Examples of trihydric and higher alcohols include those having 3 to 24 carbon atoms, such as glycerol, diglycerol, sorbitol, and stachyose. Especially preferred alcohols are di- to hexahydric alcohols having 2 to 6 carbon atoms.

[0050] (2) Nonionic Surfactants Based on Sugar Alcohol

[0051] Examples of the nonionic surfactants based on a sugar alcohol (2) include sugar alcohol/AO adducts, fatty acid esters of sugar alcohol/AO adducts, and fatty acid esters of sugar alcohols. The sugar alcohol as a component of a nonionic surfactant based on a polyhydric alcohol is an alcohol obtained from a monosaccharide having 3 to 6 carbon atoms through reduction of the aldehyde or ketone group. Examples thereof include glycerol, erythritol, arabitol, sorbitol, and mannitol. Especially preferred are those having 6 carbon atoms. The fatty acid as a component of the fatty acid ester in a sugar alcohol/AO adduct may be any of saturated and unsaturated fatty acids each having 1 to 24, preferably 12 to 18, carbon atoms. Preferred is oleic acid. With respect to the degree of esterification of the sugar alcohol, the number of OH groups which have undergone esterification may be any of from zero to all of the OH groups. However, the degree of esterification is preferably 1 to 3. The kinds of AO and the average number of moles of AO added are the same as in (1)

[0052] (3) Nonionic Surfactants Based on Sugar

[0053] Examples of the nonionic surfactants based on a sugar (3) include sugar/AO adducts, fatty acid esters of sugar/AO adducts, and sugar/fatty acid esters. The sugar may be a polysaccharide such as sucrose, besides any of the monosaccharides mentioned above with regard to the sugar alcohol. Preferred are glucose and sucrose. The kinds of AO and the average number of moles of AO added are the same as in (1). Especially preferred of the nonionic surfactants based on a sugar (3) are sugar/AO adducts, in particular, glucose/PO adducts in which the average number of moles of PO added is 1 to 10.

[0054] When at least one compound (i) selected among cationic compounds, amine compounds, acid salts of amine compounds, amphoteric compounds, amide compounds, quaternary ammonium salts, and imidazoline derivatives is used in combination with at least one nonionic surfactant (ii) such as the compounds (A) to (C) described above, the proportion of the compound (i) to the nonionic surfactant (ii) is from 100/0 to 1/99, preferably from 100/0 to 10/90 by weight.

[0055] The compounds (i) and (ii) maybe added either as a mixture of both or separately.

[0056] The bulking promoter of this invention is applicable to a variety of ordinary pulp feedstocks ranging from virgin pulps such as mechanical pulps and chemical pulps to pulps prepared (deinked) from various waste papers. The point where the bulking promoter of this invention is added is not particularly limited as long as it is within the papermaking process steps. In a factory, for example, the bulking promoter is desirably added at a point where it can be evenly blended with a pulp feedstock, such as, the refiner, machine chest, or headbox. After the bulking promoter of this invention is added to a pulp feedstock, the resultant mixture is subjected as it is to sheet forming. The bulking promoter remains in the paper. The paper bulking promoter of this invention is added in an amount of 0.01 to 10 wt. %, preferably 0.1 to 5 wt. %, based on the pulp.

[0057] The pulp sheet obtained by using the paper bulking promoter of this invention has a bulk density (the measurement method is shown in the Examples given later) lower by desirably at least 5%, preferably at least 7% than the product not containing the paper bulking promoter and has a tearing strength as measured according to JIS P 8116 of desirably at least 90%, preferably at least 95% of that of the product.

EXAMPLES

[0058] This invention will be explained below in more detail by reference to Examples, but the invention should not be construed as being limited thereto. In the Examples, all parts and percents are based on weight unless otherwise indicated.

[0059] When the unit number of an (AO) group is defined by an integer, the compound is one of a mixture of reaction products. When it is defined by an average value, the compound is a mixture of reaction products.

Examples 1 to 42 and Comparative Example 1

[0060] [Pulp Feedstocks]

[0061] The deinked pulp and virgin pulp shown below were used as pulp feedstocks.

[0062] <Deinked Pulp>

[0063] A deinked pulp was obtained in the following manner. To feedstock waste papers collected in the city (newspaper/leaflet=70/30%) were added warm water, 1% (based on the feedstock) of sodium hydroxide, 3% (based on the feedstock) of sodium silicate, 3% (based on the feedstock) of a 30% aqueous hydrogen peroxide solution, and 0.3% (based on the feedstock) of EO/PO block adduct of beef tallow/glycerol (1:1), as a deinking agent, in which the amounts of EO and PO were respectively 70 and 10 (average number of moles added). The feedstock was disintegrated and then subjected to flotation. The resultant slurry was washed with water and regulated to a concentration of 1% to prepare a deinked pulp (DIP) slurry. This DIP had a freeness of 220 ml.

[0064] <Virgin Pulp>

[0065] A virgin pulp was prepared by disintegrating and beating an LBKP (bleached hardwood pulp) with a beater at room temperature to give a 1% LBKP slurry. This LBKP had a freeness of 420 ml.

[0066] [Bulking Promoters]

[0067] The cationic compounds, amine compounds, acids salts of amine compounds, and amphoteric compounds shown in Tables 1 to 5 were used optionally together with the nonionic surfactants shown in Table 6 in the combinations shown in Tables 7 and 8, which will be given later. TABLE 1 Compound Structure in the formula (a1) No. R¹¹ R¹² R¹³ R¹⁴ X⁻ Cationic compound A-1 C18 C18 C1 C1 Cl⁻ A-2 C12 C14 C1 C1 Cl⁻ a-1 C2 C2 C1 C1 Cl⁻ a-2 C4 C4 C1 C1 Br⁻

[0068] TABLE 2 Compound Structure in the formula (b1) No. R¹³ R¹⁴ R¹⁵ R¹⁶ X⁻ Cationic compound B-1 C1 C1 C1 C12 Cl⁻ B-2 C1 C1 C1 C16 Br⁻ B-3 C1 C1 C1 C18 Cl⁻ B-4 benzyl C1 C1 C12 Cl⁻ b-1 C1 C1 C1 C2 Cl⁻ b-2 C1 C1 C1 C4 Br⁻

[0069] TABLE 3 Compound Structure in the formula (a2) or (b₂₎ No. R₂₁ R₂₂ R₂₃ HB Amine compound and acid salt of amine compound C-1 C12 H H — C-2 C18 H H — C-3 C16/C18 = C16/C18 = H — 3/7 3/7 C-4 C18 C1 C1 — c-1 C4 H H — c-2 C6 H H — c-3 C2 C2 H — c-4 C4 C1 C1 — C-5 C16/C18 = H H CH₃COOH 3/7 c-5 C4 H H CH₃COOH

[0070] TABLE 4 Structure in the formula (a₃) Compound No. R₃₁ R₃₂ R₃₃ Amphoteric D-1 C12 C1 C1 compound d-1 C4 C1 C1

[0071] TABLE 5 Structure in the formula (b₃) Compound No. R₃₁ R₃₂ R₃₃ Amphoteric D-2 C12 C1 C1 compound D-3 C18 C1 C1 d-2 C6 C1 C1

[0072] TABLE 6 (1)/(2)/ (3) Nonionic surfactant Weight No. (1) (2) (3) ratio 1 C12 alcohol 100/0/0 2 C12/C14 alcohol = 100/0/0 5/5 PO = 5 3 Beef tallow/fatty 100/0/0 acid, PO = 5 4 Methyl laurate, 100/0/0 EO2/PO3 block 5 Coconut 100/0/0 oil/glycerol = 1/1, EO2/PO10 block 6 Sorbitan monoo- 100/0/0 leate. EO20 7 Dobanol23 Sorbitan 75/25/0 EO2/PO4 random monooleate, EO10 8 C12 alcohol Sorbitan Hardened 80/15/5 monooleate, EO15 castor oil, EO25 9 C18 alcohol, 100/0/0 PO = 10 10 Castor oil/fatty acid, 100/0/0 EO5/PO15 random 11 C12/C14/C18 C12 alcohol EO = 5 Fish oil/ 75/15/ alcohol = 6/2/2, sorbitol = 10 PO = 10 1/1, PO = 15 12 Beef tallow/ 100/0/0 glycerol = 1/0.3 EO10/PO10 block 13 Sorbitan mono- 100/0/0 laurate, EO15 14 C12/C14/C18 lauric acid EO5, 90/10/0 alcohol = 60/30/10, PO25 PO20 15 C12/C14 alcohol = 100/0/0 70/30 16 Lauric acid/stearic 100/0/0 acid = 50/50, PO = 18 17 Dobanol23, PO = 2 lauric acid/myristic Sorbitan 70/15/ acid/palmitic acid = trioleate EO6 15 70/20/10, EO10, PO20

[0073] (Note) In the table, Cn means an alkyl group having n carbon atoms. In Table 6, each fat/polyhydric alcohol ratio is by mole, and the other ratios are by weight. EO and PO mean ethylene oxide and propylene oxide, respectively, and the numbers following these are the average numbers of moles added. “Dobanol 23” is an alcohol manufactured by Mitsubishi Chemical.

[0074] [Papermaking Method]

[0075] Each of the above 1% pulp slurries was weighed out in such an amount as to result in a sheet of paper having a basis weight of 60 g/m². The pH thereof was adjusted to 4.5 with aluminum sulfate. Subsequently, various bulking promoters shown in Tables 7 and 8 were added in an amount of 3% based on the pulp. Each resultant mixture was formed into a sheet with a rectangular TAPPI paper machine using an 80-mesh wire. The sheet obtained was pressed with a press at 3.5 kg/cm² for 2 minutes and dried with a drum dryer at 105° C. for 1 minute. After each dried sheet was held under the conditions of 20° C. and a humidity of 65% for 1 day to regulate its moisture content, it was evaluated for bulk density as a measure of paper bulkiness and for tearing strength as a measure of paper strength performance. The results obtained are shown in Tables 7 and 8. Ten found values were averaged.

[0076] <Evaluation Item and Method>

[0077] Bulkiness (Bulk Density)

[0078] The basis weight (g/m²) and thickness (mm) of each sheet having a regulatedmoisture contentweremeasured, and its bulk density (g/cm³) was determined as a calculated value.

[0079] Equation for calculation:

Bulkiness (bulk density)=(basis weight)/(thickness)×0.001

[0080] The smaller the absolute value of bulk density, the higher the bulkiness. A difference of 0.02 in bulk density is sufficiently recognized as a significant difference.

[0081] Paper Strength (Tearing Strength)

[0082] Each sheet having a regulated moisture content was examined according to JIS P 8116 (Testing Method for Tearing Strength of Paper and Paperboard).

[0083] Equation for calculation:

Tearing strength=A/S×16

[0084] Tearing strength: (gf)

[0085] A: Reading

[0086] S: Number of torn sheets

[0087] The larger the absolute value of tearing strength, the higher the paper strength. A difference of 20 gf in tearing strength is sufficiently recognized as a significant difference. TABLE 7 Cationic compound, amine compound, acid Nonionic Deinked salt of amine surfactant Pulp LBKP compound, used in (i)/(ii) Bulk Tearing Bulk Tearing amphoteric combination weight density strength density strength Example compound (i) (ii) ratio (g/cm³) (gf) (g/cm³) (gf)  1 B-1 none — 0.330 420 0.377 480  2 B-2 ↑ — 0.328 420 0.376 480  3 B-3 ↑ — 0.325 415 0.374 475  4 B-4 ↑ — 0.330 415 0.378 480  S A-1 ↑ — 0.325 420 0.375 475  6 A-2 ↑ — 0.330 420 0.377 480  7 C-1 ↑ — 0.342 430 0.385 485  8 C-2 ↑ — 0.340 430 0.383 485  9 B-3 ↑ — 0.338 425 0.383 480 10 B-4 ↑ — 0.335 420 0.379 480 11 C-5 ↑ — 0.332 420 0.377 480 12 D-1 ↑ — 0.331 415 0.377 475 13 D-2 ↑ — 0.331 415 0.377 475 14 D-3 ↑ — 0.328 420 0.375 475 15 B-1  1 20/80 0.313 410 0.349 470 16 B-3  2 30/70 0.308 400 0.342 460 17 B-3  3 50/50 0.309 405 0.344 455 18 B-3  4 85/15 0.312 410 0.346 460 19 B-3  5 90/10 0.314 410 0.349 465 20 A-1  6 85/15 0.309 400 0.345 460 21 B-4  7 30/70 0.310 405 0.345 455 22 B-3  8 20/80 0.308 400 0.341 460 23 C-2  9 65/35 0.324 410 0.360 470 24 C-3 10 80/20 0.323 415 0.358 470 25 C-4 11 10/90 0.317 415 0.355 465 26 C-5 12 70/30 0.321 410 0.357 465 27 C-5 13 55/45 0.322 415 0.357 470 28 C-5 14 20/80 0.319 415 0.356 465 29 D-1 15 15/85 0.314 410 0.348 460 30 D-3 16 80/20 0.312 405 0.345 460 31 D-3 17 35/65 0.308 400 0.342 455

[0088] TABLE 8 Cationic compound, amine compound, acid Deinked salt of amine Nonionic pulp LBKP compound, surfactant Bulk Tearing Bulk Tearing amphoteric used in density strength density strength Example compound (i) combination (ii) (g/cm³) (gf) (g/cm³) (gf) 32 b-1 none 0.366 440 0.405 495 33 b-2 ↑ 0.365 440 0.402 485 34 a-1 ↑ 0.365 435 0.404 490 35 a-2 ↑ 0.366 430 0.405 490 36 c-1 ↑ 0.367 435 0.404 495 37 c-2 ↑ 0.368 430 0.407 490 38 c-3 ↑ 0.365 425 0.404 490 39 c-4 ↑ 0.365 435 0.403 485 40 c-5 ↑ 0.366 430 0.405 490 41 d-1 ↑ 0.364 440 0.404 495 42 d-2 ↑ 0.363 430 0.406 490 Control (no bulking promoter) 0.375 430 0.414 490 Comparative example 1 0.330 280 0.379 345 

1. A process for producing a bulky paper, comprising the step of making paper from pulp in the presence of a bulking promoter omprising at least one compound selected from the group consisting of a cationic compound, an amine compound, an acid salt of an amine compound, an amphoteric compound, an amide compound and an imidazoline derivative,.
 2. The process as claimed in claim 1, wherein the cationic compound is a compound represented by the following formula (a₁) or (b₁):

wherein R₁₁ and R₁₂ are the same as or different from each other, and an alkyl, alkenyl or β-hydroxyalkyl group having 8 to 24 carbon atoms; R₁₃, R₁₄ and R₁₅ are the same as or different from each other, and an alkyl or hydroxyalkyl group having 1 to 8 carbon atoms, benzyl or —(AO)n₁₁—Z₁₁, wherein AO is an oxyalkylene unit having 2 or 3 carbon atoms, Z₁₁ is a hydrogen atom or an acyl group and n₁₁ is an integer of 1 to 50; R₁₆ is an alkyl, an alkenyl or β-hydroxyalkyl group having 8 to 36 carbon atoms; and X is an anionic ion.
 3. The process as claimed in claim 1, wherein the amine compound and an acid salt of an amine compound are compounds represented by the following formulae (a₂) to (f₂):

wherein R₂₁ is an alkyl, alkenyl or β-hydroxyalkyl group having 8 to 36 carbon atoms; R₂₂ and R₂₃ are the same as or different from each other, and a hydrogen atom, an alkyl group having 1 to 24 carbon atoms or an alkenyl group having 2 to 24 carbon atoms; R₂₄ and R₂, are the same as or different from each other, and a hydrogen atom or an alkyl group having 1 to 3 carbon atoms; HB represents an inorganic acid or an organic acid; AO is an oxyalkylene unit having 2 or 3 carbon atoms; l₂₁ and m₂₁ are 0 or a positive integer, and the sum in total of l₂₁ and m₂₁ is in an integer ranging from 1 to 300; and n₂₁ is a number of 1 to
 4. 4. The process as claimed in claim 1, wherein the amphoteric compound is a compound represented by the following formula (a₃) to (j3):

wherein R₃₁, R₃₂ and R₃₃ are the same as or different from each other, and an alkyl group having 1 to 24 carbon atoms or an alkenyl group having 2 to 24 carbon atoms; R₃₄ is an alkyl, alkenyl or β-hydroxyalkyl group having 8 to 36 carbon atoms; M is a hydrogen atom, an alkali metal atom, a half a mole of an alkaline earth metal atom or an ammonium group; Y₃₁ is R₃₅NHCH₂CH₂—, wherein R₃₅ is an alkyl group having 1 to 36 carbon atoms, or an alkenyl or a hydroxy alkyl group having 2 to 36 carbon atoms; Y₃₂ is a hydrogen atom or R₃₅NHCH₂CH₂—, R₃₅ being defined above; Z₃₁ is —CH₂COOM, M being defined above; and Z₃₂ is a hydrogen atom or —CH₂COOM, M being defined above.
 5. The process as claimed in claim 1, wherein the amine compound and acid salt of an amine compound are compounds represented by the following formulae (a₄) to (d₄):

wherein R₄₁ is an alkyl, alkenyl or β-hydroxyalkyl group having 8 to 35 carbon atoms; R₄₃ and R₄₄ are same as or different from each other, an alkyl, alkenyl or β-hydroxyalkyl group having 7 to 35 carbons atoms; R₄₆ is a hydrogen atom or an alkyl group having 1 to 3 carbon atoms; R₄₅ is an alkyl group having 1 to 3 carbon atoms; R₄₂ is a hydrogen atom or R₄₇, R₄₇ being an alkyl, alkenyl or β-hydroxyalkyl group having 7 to 35 carbons atoms; Y₄₁ is a hydrogen atom or —COR₄₄; and Z₄₁ is —CH₂CH₂O(AO)n₄₁—OCOR₄₇, wherein A is a liner or branched alkylene unit having 2 to 3 carbon atoms and n₄₁ is an average added-number ranging 1 to 20, or —CH₂CH(OH)—CH₂OCOR₄₇.
 6. The process as claimed in claim 1, wherein the amide compound is represented by the following formulae (a₅) and (b₅):

wherein R₅₁ and R₅₄ are same as or different from each other, an alkyl, alkenyl or β-hydroxyalkyl group having 7 to 35 carbon atoms; R₅₂ and R₅₃ are same as or different from each other, a hydrogen atom or an alkyl group having 1 to 3 carbon atoms; and Y₅₁ and Y₅₂ are same as or different from each other, and a hydrogen atom, R₅₂CO—, R₅₄CO—, —(AO)n₅₁—COR₅₅, wherein A is a liner or branched alkylene unit having 2 to 3 carbon atoms n₅₁ is an average added number ranging 1 to 20, and R₅₅ is an alkyl, alkenyl or β-hydroxyalkyl group having 7 to 35 carbon atoms, or —(AO)n₅₁—H, A and n₅₁ being defined above.
 7. The process as claimed in claim 1, wherein the cationic compound is a quaternary ammonium salt represented by the following formulae (a₆) and (b₆):

wherein R₆₁ and R₆₃ are same as or different from each other, an alkyl, alkenyl or β-hydroxyalkyl group having 7 to 35 carbons atoms; R₆₅ is a hydrogen atom or an alkyl group having 1 to 3 carbon atoms; R₆₂ and R₆₄ are same as or different from each other, an alkyl group having 1 to 3 carbon atoms; and X⁻ is an anionic ion.
 8. The process as claimed in claim 1, wherein the imidazoline derivative is a compound represented by the formula (h):

wherein R₇₁ is an alkyl, alkenyl or β-hydroxyalkyl group having 7 to 35 carbons atoms.
 9. The process as claimed in any of claims 1 to 9, which further comprises at least one of the nonionic surfactants represented by the following formulae (A) to (C); (A): a compound represented by the following formula (A) R₈₁O(EO)_(m) ₈₁ (PO)_(n) ₈₁ H  (A) wherein R₈₁ is a C6 to C22 straight or branched alkyl or alkenyl group or an alkylaryl group having a C4 to C20 alkyl group; E is an ethylene unit; P is a propylene unit; m₈₁ and n₈₁ are an average number of added moles, m₈₁ is a number in the range of 0 to 20 and n₈₁ is a number in the range of 0 to 50; and the addition form of EO and PO may be any of block and random and the addition order of EO and PO may be not limited; (B): a compound represented by the following formula (B) R₈₁COO(EO)_(m) ₈₁ (PO)_(n) ₈₁ R_(b)  (B) wherein R₈₁, E, P, m₈₁ and n₈₁ are the same as those of the formula (A); and R_(b) is H, an alkyl group, an alkenyl group or an alkylaryl group; (C): a nonionic surfactant selected from the followings (1) to (3): (1) an oil-fat type nonionic surfactant, (2) a sugar-alcohol type nonionic surfactant and (3) a sugar-type nonionic surfactant.
 10. A method for bulking paper with the bulking promoter as defined in claim
 1. 